Canonical Allele Identifier: CA783245115
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs60181927

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11108243dup , CM000681.2:g.11108243dup GRCh38
NC_000019.9:g.11218919dup , CM000681.1:g.11218919dup GRCh37
NC_000019.8:g.11079919dup NCBI36
NG_009060.1:g.23863dup , LRG_274:g.23863dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1198+729dup ENSP00000252444.6:n.1198+729dup
ENST00000559340.2:c.940+729dup ENSP00000453696.2:n.940+729dup
ENST00000560467.2:c.940+729dup ENSP00000453513.2:n.940+729dup
ENST00000558518.6:c.940+729dup MANE Select ENSP00000454071.1:n.940+729dup
ENST00000252444.9:c.1194+729dup
ENST00000455727.6:c.436+729dup ENSP00000397829.2:n.436+729dup
ENST00000535915.5:c.817+729dup ENSP00000440520.1:n.817+729dup
ENST00000545707.5:c.559+729dup ENSP00000437639.1:n.559+729dup
ENST00000557933.5:c.940+729dup ENSP00000453557.1:n.940+729dup
ENST00000558013.5:c.940+729dup ENSP00000453346.1:n.940+729dup
ENST00000558518.5:c.940+729dup ENSP00000454071.1:n.940+729dup
ENST00000560467.1:c.540+729dup
NM_000527.4:c.940+729dup , LRG_274t1:c.940+729dup NP_000518.1:n.940+729dup
NM_001195798.1:c.940+729dup NP_001182727.1:n.940+729dup
NM_001195799.1:c.817+729dup NP_001182728.1:n.817+729dup
NM_001195800.1:c.436+729dup NP_001182729.1:n.436+729dup
NM_001195803.1:c.559+729dup NP_001182732.1:n.559+729dup
XM_011528010.1:c.940+729dup XP_011526312.1:n.940+729dup
XM_011528011.1:c.559+729dup XP_011526313.1:n.559+729dup
XR_244074.2:n.1090+729dup
XM_011528010.2:c.940+729dup XP_011526312.1:n.940+729dup
XR_001753685.2:n.1057+729dup
XR_001753686.2:n.1057+729dup
NM_000527.5:c.940+729dup MANE Select NP_000518.1:n.940+729dup
NM_001195798.2:c.940+729dup NP_001182727.1:n.940+729dup
NM_001195799.2:c.817+729dup NP_001182728.1:n.817+729dup
NM_001195800.2:c.436+729dup NP_001182729.1:n.436+729dup
NM_001195803.2:c.559+729dup NP_001182732.1:n.559+729dup